Db	Link	Name	Definition	Comment	Is a
OMIM	OMIM:616897	OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE; OCLSBG	—	—	—
OMIM	OMIM:616898	CHROMOSOME 15q14 DELETION SYNDROME	—	—	—
OMIM	OMIM:616900	HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION AND CHARACTERISTIC FACIES 3; IHPRF3	—	—	—
OMIM	OMIM:616901	DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FEATURES, AND SPARSE HAIR; DEDSSH	—	—	—
OMIM	OMIM:616902	CHROMOSOME 11p13 DELETION SYNDROME, DISTAL	—	—	—
OMIM	OMIM:616903	THIOPURINES, POOR METABOLISM OF, 2; THPM2	—	—	—
OMIM	OMIM:616907	SPASTIC PARAPLEGIA 76, AUTOSOMAL RECESSIVE; SPG76	—	—	—
OMIM	OMIM:616910	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 3; ICF3	—	—	—
OMIM	OMIM:616911	IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 4; ICF4	—	—	—
OMIM	OMIM:616913	BLEEDING DISORDER, PLATELET-TYPE, 20; BDPLT20	—	—	—
OMIM	OMIM:616914	MARFAN LIPODYSTROPHY SYNDROME; MFLS	—	—	—
OMIM	OMIM:616917	MENTAL RETARDATION, AUTOSOMAL RECESSIVE 53; MRT53	—	—	—
OMIM	OMIM:616920	HEART AND BRAIN MALFORMATION SYNDROME; HBMS	—	—	—
OMIM	OMIM:616921	DYSKINESIA, LIMB AND OROFACIAL, INFANTILE-ONSET; IOLOD	—	—	—
OMIM	OMIM:616922	STRIATAL DEGENERATION, AUTOSOMAL DOMINANT 2; ADSD2	—	—	—
OMIM	OMIM:616924	CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2CC; CMT2CC	—	—	—
OMIM	OMIM:616937	THROMBOCYTOPENIA 6; THC6	—	—	—
OMIM	OMIM:616938	COFFIN-SIRIS SYNDROME 5; CSS5	—	—	—
OMIM	OMIM:616939	CHOREA, CHILDHOOD-ONSET, WITH PSYCHOMOTOR RETARDATION; COCPMR	—	—	—
OMIM	OMIM:616941	AGAMMAGLOBULINEMIA 8, AUTOSOMAL DOMINANT; AGM8	—	—	—
OMIM	OMIM:616943	TRICHOTHIODYSTROPHY 6, NONPHOTOSENSITIVE; TTD6	—	—	—
OMIM	OMIM:616944	MENTAL RETARDATION, AUTOSOMAL DOMINANT 41; MRD41	—	—	—
OMIM	OMIM:616946	PREMATURE OVARIAN FAILURE 11; POF11	—	—	—
OMIM	OMIM:616947	PREMATURE OVARIAN FAILURE 12; POF12	—	—	—
OMIM	OMIM:616948	SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 22; SCAR22	—	—	—